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      High resolution ultrasonic neural modulation observed via in vivo two-photon calcium imaging

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          Abstract

          Neural modulation plays a major role in delineating the circuit mechanisms and serves as the cornerstone of neural interface technologies. Among the various modulation mechanisms, ultrasound enables noninvasive label-free deep access to mammalian brain tissue. To date, most if not all ultrasonic neural modulation implementations are based on ~1 MHz carrier frequency. The long acoustic wavelength results in a spatially coarse modulation zone, often spanning over multiple function regions. The modulation of one function region is inevitably linked with the modulation of its neighboring regions. Moreover, the lack of in vivo cellular resolution cell-type-specific recording capabilities in most studies prevents the revealing of the genuine cellular response to ultrasound. To significantly increase the spatial resolution, we explored the application of high-frequency ultrasound. To investigate the neuronal response at cellular resolutions, we developed a dual-modality system combining in vivo two-photon calcium imaging and focused ultrasound modulation. The studies show that the ~30 MHz ultrasound can suppress the neuronal activity in awake mice at 100-mm scale spatial resolutions, paving the way for high-resolution ultrasonic neural modulation. The dual-modality in vivo system validated through this study will serve as a general platform for studying the dynamics of various cell types in response to ultrasound.

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          Transcranial pulsed ultrasound stimulates intact brain circuits.

          Electromagnetic-based methods of stimulating brain activity require invasive procedures or have other limitations. Deep-brain stimulation requires surgically implanted electrodes. Transcranial magnetic stimulation does not require surgery, but suffers from low spatial resolution. Optogenetic-based approaches have unrivaled spatial precision, but require genetic manipulation. In search of a potential solution to these limitations, we began investigating the influence of transcranial pulsed ultrasound on neuronal activity in the intact mouse brain. In motor cortex, ultrasound-stimulated neuronal activity was sufficient to evoke motor behaviors. Deeper in subcortical circuits, we used targeted transcranial ultrasound to stimulate neuronal activity and synchronous oscillations in the intact hippocampus. We found that ultrasound triggers TTX-sensitive neuronal activity in the absence of a rise in brain temperature (<0.01 degrees C). Here, we also report that transcranial pulsed ultrasound for intact brain circuit stimulation has a lateral spatial resolution of approximately 2 mm and does not require exogenous factors or surgical invasion. Copyright 2010 Elsevier Inc. All rights reserved.
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            Transcranial magnetic stimulation: a primer.

            Transcranial magnetic stimulation (TMS) is a technique for noninvasive stimulation of the human brain. Stimulation is produced by generating a brief, high-intensity magnetic field by passing a brief electric current through a magnetic coil. The field can excite or inhibit a small area of brain below the coil. All parts of the brain just beneath the skull can be influenced, but most studies have been of the motor cortex where a focal muscle twitch can be produced, called the motor-evoked potential. The technique can be used to map brain function and explore the excitability of different regions. Brief interference has allowed mapping of many sensory, motor, and cognitive functions. TMS has some clinical utility, and, because it can influence brain function if delivered repetitively, it is being developed for various therapeutic purposes.
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              Optogenetics.

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                Author and article information

                Journal
                101465726
                35618
                Brain Stimul
                Brain Stimul
                Brain stimulation
                1935-861X
                1876-4754
                10 January 2022
                Jan-Feb 2022
                21 December 2021
                06 June 2022
                : 15
                : 1
                : 190-196
                Affiliations
                [a ]School of Electrical and Computer Engineering, Purdue University, West Lafayette, IN, 47907, USA
                [b ]Bindley Bioscience Center, Purdue University, West Lafayette, IN, 47907, USA
                [c ]Skirball Institute, Department of Neuroscience and Physiology, Department of Anesthesiology, New York University School of Medicine, New York, NY, 10016, USA
                [d ]Department of Biomedical Engineering and Department of Ophthalmology, University of Southern California, Los Angeles, CA, 90089, USA
                [e ]Department of Biology, Purdue University, West Lafayette, IN, 47907, USA
                Author notes
                [* ]Corresponding author. School of Electrical and Computer Engineering, Purdue University, West Lafayette, IN, 47907, USA. mengcui@ 123456purdue.edu (M. Cui). Correspondence and requests for materials should be addressed to M.C.
                Article
                NIHMS1767169
                10.1016/j.brs.2021.12.005
                9169577
                34952226
                825834ca-70c9-4c27-96c9-22d6f3072bce

                This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/).

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                Neurosciences
                Neurosciences

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